Literature DB >> 29572974

Impact of remnant vital tissue after locoregional treatment and liver transplant in hepatocellular cancer patients, a multicentre cohort study.

Tommaso M Manzia1, Quirino Lai2, Samuele Iesari3, M Thamara P R Perera4, Mina Komuta3, Amanda Carvalheiro4, Tahir Shah4, Roberta Angelico4,5, Claudia Quaranta1, Daniele Nicolini6, Roberto Montalti6, Marina Scarpelli6, Giampiero Palmieri7, Antonio Orlacchio7, Marco Vivarelli6, Mario Angelico1, Jan Lerut3, Giuseppe Tisone1.   

Abstract

The role of pathological findings after locoregional treatments as predictors of hepatocellular cancer recurrence after liver transplantation has been poorly addressed. The aim of the study was to identify the role of remnant vital tissue (RVT) of the target lesion in predicting hepatocellular cancer recurrence. Two hundred and seventy-six patients firstly undergoing locoregional treatment and then transplanted between January 2010 and December 2015 in four European Transplant Centres (i.e. Rome Tor Vergata, Birmingham, Brussels and Ancona) were enrolled in the study to investigate the role of pathological response at upfront locoregional treatment. At multivariable Cox regression analysis, RVT ≥2 cm was a strong independent risk factor for post-LT recurrence (HR = 5.6; P < 0.0001). Five-year disease-free survival rates were 60.8%, 80.9% and 95.0% in patients presenting a RVT ≥2 cm vs. 0.1-1.9 vs. no RVT, respectively. When only Milan Criteria-IN patients were analysed, similar results were reported, with 5-year disease-free survival rates of 58.1%, 79.0% and 94.0% in patients presenting a RVT ≥2 cm vs. 0.1-1.9 vs. no RVT, respectively. RVT is an important determinant of tumour recurrence after liver transplantation performed for hepatocellular cancer. Its discriminative power looks to be evident also in a Milan-IN setting, suggesting to more liberally use locoregional treatments also in these patients.
© 2018 Steunstichting ESOT.

Entities:  

Keywords:  Milan Criteria; hepatocellular carcinoma; liver transplantation; locoregional treatment; recurrence

Year:  2018        PMID: 29572974     DOI: 10.1111/tri.13153

Source DB:  PubMed          Journal:  Transpl Int        ISSN: 0934-0874            Impact factor:   3.782


  6 in total

1.  Liver transplantation for hepatocellular carcinoma: pushing the boundaries.

Authors:  Joanne M O'Rourke; Shishir Shetty; Tahir Shah; M Thamara P R Perera
Journal:  Transl Gastroenterol Hepatol       Date:  2019-01-02

Review 2.  Hepatocellular carcinoma in children: hepatic resection and liver transplantation.

Authors:  Roberta Angelico; Chiara Grimaldi; Maria Cristina Saffioti; Aurora Castellano; Marco Spada
Journal:  Transl Gastroenterol Hepatol       Date:  2018-09-10

3.  Locoregional therapy response in patients with hepatocellular cancer waiting for liver transplantation: Only selection or biological effect?

Authors:  Quirino Lai; Michele Di Martino; Pierleone Lucatelli; Gianluca Mennini
Journal:  World J Gastroenterol       Date:  2018-08-21       Impact factor: 5.742

4.  Stereotactic Radiofrequency Ablation of Hepatocellular Carcinoma: a Histopathological Study in Explanted Livers.

Authors:  Reto Bale; Peter Schullian; Gernot Eberle; Daniel Putzer; Heinz Zoller; Stefan Schneeberger; Claudia Manzl; Patrizia Moser; Georg Oberhuber
Journal:  Hepatology       Date:  2019-02-14       Impact factor: 17.425

5.  Clinical Outcomes of Patients With Unresectable Primary Liver Cancer Treated With Yttrium-90 Radioembolization With an Escalated Dose.

Authors:  Re-I Chin; Anirudh Bommireddy; Tyler J Fraum; Daniel R Ludwig; Yi Huang; Jacqueline E Zoberi; Jose L Garcia-Ramirez; Nichole M Maughan; William Chapman; Kevin Korenblat; Lauren E Henke; Hyun Kim; Shahed N Badiyan
Journal:  Adv Radiat Oncol       Date:  2022-03-21

Review 6.  Upper Limits of Downstaging for Hepatocellular Carcinoma in Liver Transplantation.

Authors:  Marco Biolato; Tiziano Galasso; Giuseppe Marrone; Luca Miele; Antonio Grieco
Journal:  Cancers (Basel)       Date:  2021-12-17       Impact factor: 6.639

  6 in total

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